Reagent condition is needed to be explained for the given reactions. Concept introduction: Acid-catalyzed reaction: in this reaction, double bond of the alkene is protonated by an acid to give carbocation intermediate that means carbocation stability determines the reactivity level of the alkene. More reactive alkene is one, which can produce more stable carbocation. If the substrate contained good leaving group then dilute sulfuric acid is enough to remove the group but in case of bad leaving group, concentrated sulfuric acid is needed to remove the group. In both the reactions first protonation of substrate takes place then attack of nucleophile leads the product. To find: the nature of the reagent in given reaction.

Question

Want to see the full answer?

Answer 1

Question

Chapter 8.5, Problem 9CC

(a)

Interpretation Introduction

Interpretation:

Reagent condition is needed to be explained for the given reactions.

Concept introduction:

Acid-catalyzed reaction: in this reaction, double bond of the alkene is protonated by an acid to give carbocation intermediate that means carbocation stability determines the reactivity level of the alkene. More reactive alkene is one, which can produce more stable carbocation.

If the substrate contained good leaving group then dilute sulfuric acid is enough to remove the group but in case of bad leaving group, concentrated sulfuric acid is needed to remove the group. In both the reactions first protonation of substrate takes place then attack of nucleophile leads the product.

To find: the nature of the reagent in given reaction.

(b)

Interpretation Introduction

Interpretation:

Reagent condition is needed to be explained for the given reactions.

Concept introduction:

Acid-catalyzed reaction: in this reaction, double bond of the alkene is protonated by an acid to give carbocation intermediate that means carbocation stability determines the reactivity level of the alkene. More reactive alkene is one, which can produce more stable carbocation.

If the substrate contained good leaving group then dilute sulfuric acid is enough to remove the group but in case of bad leaving group, concentrated sulfuric acid is needed to remove the group. In both the reactions first protonation of substrate takes place then attack of nucleophile leads the product.

To find: the nature of the reagent in given reaction.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Formulate the products obtained by reacting p-toluidine with a sulfonate mixture. Indicate the majority if necessary.

Consider this organic reaction: OH Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significant rate, check the box under the drawing area instead. Click and drag to start drawing a structure. x 0: の C

Explain the reasons for a compound's greater or lesser reactivity toward electrophilic aromatic substitution. Give reasons.